A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985335



Internal ID57631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89136173..89141974hg38UCSC Ensembl
chr6:89845892..89851693hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg385802
hg195802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467781
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985335
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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